regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143209557 | T | TAAAAA | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0021others(21): Show | 24 | 162 | 0.1482 | 5 | c.235 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | C | CAAAAA | intron_variant | MODIFIER | HG01358.hp1 HG02071.hp1 HG02723.hp1 others(11): Show |
a0001a0003 | a0001c0001a0003c0005 | a0001c0001t0001a0003c0005t0001 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0016others(11): Show | 14 | 162 | 0.0864 | 5 | c.385 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143461281 | C | CAAAAA | intron_variant | MODIFIER | HG02523.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0102others(4): Show | 7 | 162 | 0.0432 | 5 | c.703 others(24): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143495460 | T | TTTTTC | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(33): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(33): Show | 36 | 162 | 0.2222 | 5 | c.826 others(22): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143555860 | A | AAGAAT | intron_variant | MODIFIER | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0018others(23): Show | 26 | 162 | 0.1605 | 5 | c.926 others(20): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAAAA | intron_variant | MODIFIER | HG01496.hp1 HG01496.hp2 HG02071.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(5): Show | 8 | 162 | 0.0494 | 5 | c.100 others(26): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24916422 | C | CTTTTT | downstream_gene_variant | MODIFIER | HG02622.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0004a0001c0004t0002 | a0001c0001t0001g0026a0001c0001t0004g0011a0001c0001t0004g0226others(2): Show | 5 | 240 | 0.0208 | 5 | c.*37 others(16): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2966 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24961968 | G | GTTTTT | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(4): Show | 7 | 240 | 0.0292 | 5 | c.574 others(22): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24961972 | G | GTTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(72): Show |
a0001a0003 | a0001c0001a0003c0007 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(68): Show | 75 | 240 | 0.3125 | 5 | c.574 others(22): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24982997 | T | TATATA | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG01243.hp2 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0055others(13): Show | 19 | 240 | 0.0792 | 5 | c.54- others(20): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625136 | T | TATATG | intron_variant | MODIFIER | HG02451.hp1 HG02896.hp1 HG03195.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(1): Show | a0001c0001t0002g0145a0001c0001t0007g0077a0001c0001t0010g0137others(1): Show | 4 | 238 | 0.0168 | 5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625178 | T | TATTTA | intron_variant | MODIFIER | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0005a0001c0001t0009a0001c0011t0001others(1): Show | a0001c0001t0005g0212a0001c0001t0009g0069a0001c0001t0009g0071others(2): Show | 5 | 238 | 0.0210 | 5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625386 | T | TATATG | intron_variant | MODIFIER | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0001c0001t0009a0002c0002t0005 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | 238 | 0.0126 | 5 | c.786 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97250747 | A | ATATAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(25): Show | a0001c0001t0001g0107a0001c0001t0001g0111a0001c0001t0001g0112others(226): Show | 229 | 242 | 0.9463 | 5 | c.928 others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97251539 | A | AAGGGG | intron_variant | MODIFIER | NA19012.hp2 NA19064.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0189a0001c0001t0001g0200 | 2 | 242 | 0.0083 | 5 | c.927 others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97259828 | C | CTGTTT | intron_variant | MODIFIER | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(5): Show | 8 | 242 | 0.0331 | 5 | c.614 others(20): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110711005 | C | CAAAAA | intron_variant | MODIFIER | HG00621.hp1 HG03098.hp1 HG03834.hp1 others(2): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0009t0002 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | 226 | 0.0221 | 5 | c.105 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24600132 | C | CAAAAA | intron_variant | MODIFIER | HG02129.hp2 HG02523.hp2 HG02818.hp1 others(4): Show |
a0001a0007a0017others(1): Show | a0001c0001a0007c0007a0017c0029others(1): Show | a0001c0001t0001a0007c0007t0006a0007c0007t0015others(2): Show | a0001c0001t0001g0143a0007c0007t0006g0291a0007c0007t0006g0292others(4): Show | 7 | 352 | 0.0199 | 5 | c.313 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24625050 | T | TGGGGG | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0187others(16): Show | 19 | 352 | 0.0540 | 5 | c.496 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24627464 | A | AAGGAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
a0001a0002a0004others(14): Show | a0001c0001a0001c0014a0002c0002others(20): Show | a0001c0001t0001a0001c0001t0004a0001c0014t0004others(27): Show | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(213): Show | 216 | 352 | 0.6136 | 5 | c.495 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628983 | T | TATATA | intron_variant | MODIFIER | HG00438.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0001 | a0001c0001t0002g0323a0002c0002t0001g0018a0002c0002t0001g0030others(11): Show | 14 | 352 | 0.0398 | 5 | c.495 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24631418 | A | ACTATT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
a0002a0004a0005others(9): Show | a0002c0002a0002c0015a0002c0017others(14): Show | a0002c0002t0001a0002c0002t0004a0002c0002t0007others(18): Show | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(149): Show | 152 | 352 | 0.4318 | 5 | c.441 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24660386 | T | TAAAAA | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
a0001a0002a0003others(9): Show | a0001c0001a0002c0002a0002c0017others(10): Show | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(16): Show | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0186others(105): Show | 108 | 352 | 0.3068 | 5 | c.268 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24687127 | G | GATCGC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
a0001a0002a0003others(18): Show | a0001c0001a0001c0014a0002c0002others(24): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(35): Show | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(290): Show | 293 | 352 | 0.8324 | 5 | c.64- others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48472524 | A | AAAAAT | intron_variant | MODIFIER | HG00558.hp2 HG00735.hp1 HG01069.hp2 others(35): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0005a0001c0001t0009a0001c0001t0015others(16): Show | a0001c0001t0005g0216a0001c0001t0009g0187a0001c0001t0015g0256others(34): Show | 38 | 270 | 0.1407 | 5 | c.451 others(22): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 4/9 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48530236 | C | CAAAAA | intron_variant | MODIFIER | HG01361.hp2 HG02071.hp1 HG02258.hp1 others(14): Show |
a0001a0003a0012others(1): Show | a0001c0001a0001c0003a0003c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0031a0001c0001t0001g0048a0001c0001t0001g0051others(14): Show | 17 | 270 | 0.0630 | 5 | c.322 others(24): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48539290 | C | CTTTTT | intron_variant | MODIFIER | HG02965.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
a0001 | a0001c0002a0001c0003a0001c0005 | a0001c0002t0001a0001c0002t0007a0001c0003t0006others(1): Show | a0001c0002t0001g0129a0001c0002t0007g0160a0001c0003t0006g0252others(1): Show | 4 | 270 | 0.0148 | 5 | c.322 others(24): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48539291 | A | ATTTTT | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0002a0001c0001t0003a0001c0001t0012others(2): Show | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0003g0242others(4): Show | 7 | 270 | 0.0259 | 5 | c.322 others(24): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48563187 | A | ATTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
a0001a0005a0009others(2): Show | a0001c0001a0001c0002a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(71): Show | 74 | 270 | 0.2741 | 5 | c.235 others(22): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38426550 | C | CAAAAA | upstream_gene_variant | MODIFIER | HG02895.hp1 HG02896.hp1 HG02965.hp2 others(4): Show |
a0001a0003 | a0001c0001a0003c0014 | a0001c0001t0001a0003c0014t0001 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0149others(4): Show | 7 | 309 | 0.0227 | 5 | c.-19 others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1913 | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38448858 | C | CTTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(33): Show |
a0001a0002a0003others(1): Show | a0001c0004a0001c0005a0001c0009others(10): Show | a0001c0004t0001a0001c0005t0001a0001c0005t0006others(11): Show | a0001c0004t0001g0069a0001c0004t0001g0170a0001c0004t0001g0171others(33): Show | 36 | 309 | 0.1165 | 5 | c.64- others(20): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85612792 | C | CTTTTT | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp1 HG04199.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0010others(1): Show | a0001c0001t0001g0021a0001c0002t0002g0078a0001c0003t0010g0083others(1): Show | 4 | 108 | 0.0370 | 5 | c.180 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85660794 | C | CAAAAA | intron_variant | MODIFIER | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0008a0001c0003t0011a0001c0004t0004others(2): Show | a0001c0002t0008g0052a0001c0002t0008g0053a0001c0003t0011g0087others(3): Show | 6 | 108 | 0.0556 | 5 | c.181 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85734636 | A | ATTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(20): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(20): Show | 23 | 108 | 0.2130 | 5 | c.268 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85743546 | T | TGACAG | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0046others(10): Show | 13 | 108 | 0.1204 | 5 | c.268 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85755626 | G | GTTTTT | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(13): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0032others(13): Show | 16 | 108 | 0.1482 | 5 | c.268 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85840150 | C | CCACCA | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG03486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0004 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0046others(2): Show | 5 | 108 | 0.0463 | 5 | c.269 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85856471 | C | CTTTTT | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG03486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0004 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0046others(2): Show | 5 | 108 | 0.0463 | 5 | c.269 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85894099 | T | TAAAAA | intron_variant | MODIFIER | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004a0001c0008 | a0001c0001t0001a0001c0004t0003a0001c0004t0004others(1): Show | a0001c0001t0001g0025a0001c0004t0003g0050a0001c0004t0003g0089others(3): Show | 6 | 108 | 0.0556 | 5 | c.269 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85973833 | G | GTTTTT | intron_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(29): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(29): Show | 32 | 108 | 0.2963 | 5 | c.733 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85982373 | T | TTTTTG | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
a0001 | a0001c0004a0001c0008 | a0001c0004t0003a0001c0004t0004a0001c0008t0014others(1): Show | a0001c0004t0003g0042a0001c0004t0003g0050a0001c0004t0003g0061others(6): Show | 9 | 108 | 0.0833 | 5 | c.928 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142839893 | A | AGGAGG | intron_variant | MODIFIER | HG02622.hp1 HG03130.hp2 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0033a0001c0001t0053 | a0001c0001t0005g0101a0001c0001t0033g0053a0001c0001t0053g0082 | 3 | 198 | 0.0152 | 5 | c.155 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAT | intron_variant | MODIFIER | HG01167.hp1 HG02155.hp2 HG02165.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0116a0001c0001t0002g0023a0001c0001t0003g0019others(3): Show | 6 | 198 | 0.0303 | 5 | c.487 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142947095 | T | TAAAAA | intron_variant | MODIFIER | HG00323.hp2 HG02132.hp1 HG02165.hp2 others(15): Show |
a0001 | a0001c0001a0001c0003a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0002g0043others(15): Show | 18 | 198 | 0.0909 | 5 | c.110 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949206 | A | AGAGAG | intron_variant | MODIFIER | HG01071.hp2 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0019 | a0001c0001t0004g0098a0001c0001t0019g0011 | 2 | 198 | 0.0101 | 5 | c.110 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142980352 | C | CTTTAT | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(88): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0018a0001c0001t0001g0153a0001c0001t0002g0005others(88): Show | 91 | 198 | 0.4596 | 5 | c.110 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTCTT | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(5): Show | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0003g0165others(7): Show | 10 | 198 | 0.0505 | 5 | c.153 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTTT | intron_variant | MODIFIER | HG00438.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(7): Show | a0001c0001t0002g0023a0001c0001t0002g0027a0001c0001t0002g0190others(9): Show | 12 | 198 | 0.0606 | 5 | c.153 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143106466 | C | CTTTTT | intron_variant | MODIFIER | HG02074.hp2 HG02523.hp2 HG03540.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0005a0001c0001t0016others(4): Show | a0001c0001t0001g0020a0001c0001t0005g0066a0001c0001t0016g0024others(5): Show | 8 | 198 | 0.0404 | 5 | c.153 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143142134 | C | CTTTTT | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(54): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0034others(54): Show | 57 | 198 | 0.2879 | 5 | c.183 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |